Raum D, Awdeh Z, Glass D, Yunis E, Alper C
Immunogenetics. 1981; 12(5-6):473-83.
PMID: 7216322
DOI: 10.1007/BF01561689.
Neel J, Mohrenweiser H, Meisler M
Proc Natl Acad Sci U S A. 1980; 77(10):6037-41.
PMID: 6934530
PMC: 350208.
DOI: 10.1073/pnas.77.10.6037.
Arends T, Weitkamp L, GALLANGO M, Neel J, Schultz J
Am J Hum Genet. 1970; 22(5):526-32.
PMID: 5534560
PMC: 1706608.
Walter H, Bajatzadeh M, Kellermann G, Matznetter T
Humangenetik. 1970; 10(4):298-303.
PMID: 5493233
DOI: 10.1007/BF00278766.
Shokeir M, Shreffler D
Biochem Genet. 1970; 4(4):517-28.
PMID: 5456439
DOI: 10.1007/BF00486602.
Studies on the population genetics of the ceruloplasmin polymorphism.
Bajatzadeh M, Walter H
Humangenetik. 1969; 8(2):134-6.
PMID: 5365582
DOI: 10.1007/BF00295836.
Genetic linkage studies in a Negro kindred with Norrie's disease.
Nance W, Hara S, Hansen A, Elliott J, Lewis M, Chown B
Am J Hum Genet. 1969; 21(5):423-9.
PMID: 5307229
PMC: 1706563.
Ceruloplasmin variants in mouse serum.
Meier H
Naturwissenschaften. 1971; 58(9):456-7.
PMID: 5112743
DOI: 10.1007/BF00624624.
On the population genetics of the ceruloplasmin polymorphism.
Kellermann G, Walter H
Humangenetik. 1972; 15(1):84-6.
PMID: 5046912
DOI: 10.1007/BF00273436.
Concerning the question of individual constancy and individual specificity of three serum enzyme activities (serum cholinesterase EC 3.1.1.8, ceruloplasmin EC 1.10.3.2, and alkaline phosphatase EC 3.1.3.1).
HOSENFELD D, Schroter E
Humangenetik. 1970; 9(1):38-42.
PMID: 4992331
DOI: 10.1007/BF00696012.
Inheritance of human alpha-1-acid glycoprotein (orosomucoid) variants.
Johnson A, Schmid K, Alper C
J Clin Invest. 1969; 48(12):2293-9.
PMID: 4982230
PMC: 297486.
DOI: 10.1172/JCI106195.
Exclusion of paternity: the current state of the art.
Chakraborty R, Shaw M, Schull W
Am J Hum Genet. 1974; 26(4):477-88.
PMID: 4841637
PMC: 1762594.
Genic variation within and between the three major races of man, Caucasoids, Negroids, and Mongoloids.
Nei M, ROYCHOUDHURY A
Am J Hum Genet. 1974; 26(4):421-43.
PMID: 4841634
PMC: 1762596.
Molecular pathology of ceruloplasmin.
NEIFAKH S, Vasiletz I, Shavlovsky M
Biochem Genet. 1972; 6(2):231-8.
PMID: 4199801
DOI: 10.1007/BF00486406.
Investigation of some biochemical genetic markers in four endogamous groups from Panjab (N. W. India). I. Protein and enzyme polymorphisms in serum.
Singh S, Sareen K, GOEDDE H
Humangenetik. 1974; 21(4):341-6.
PMID: 4134629
DOI: 10.1007/BF00273372.
Characterization, mapping, and expression of the human ceruloplasmin gene.
Yang F, Naylor S, Lum J, Cutshaw S, McCombs J, Naberhaus K
Proc Natl Acad Sci U S A. 1986; 83(10):3257-61.
PMID: 3486416
PMC: 323492.
DOI: 10.1073/pnas.83.10.3257.
The frequency of "rare" protein variants in Marshall islanders and other Micronesians.
Neel J, Ferrell R, CONARD R
Am J Hum Genet. 1976; 28(3):262-9.
PMID: 1266854
PMC: 1685014.
On the defect of synthesis ceruloplasmin in the liver polyribosomes in Wilson's disease.
GAITSKHOKI V, Kisselev O, Moshkov K, Puchkova L, Shavlovski M, Shulman V
Biochem Genet. 1975; 13(9-10):533-50.
PMID: 1239275
DOI: 10.1007/BF00484913.
[Quantitative determination and phenotyping of ceruloplasmin in morbus Wilson (author's transl)].
GOEDDE H, Benkmann H, Lange J, Harders H
Klin Wochenschr. 1975; 53(15):731-4.
PMID: 1219186
DOI: 10.1007/BF01468706.
Serum protein polymorphisms in four populations of Afghanistan.
Rahimi A, GOEDDE H, Flatz G, Kaifie S, Benkmann H, Delbruck H
Am J Hum Genet. 1977; 29(4):356-60.
PMID: 69400
PMC: 1685381.
